63127008: Thyroglobulin synthesis defect (disorder)

SNOMED CT Concept\Clinical finding\...

\Viscus structure finding\Goitre\Dyshormonogenic goitre\Thyroglobulin synthesis defect

\Finding of head and neck region\Finding of neck region\...

\Finding of thyroid gland\Thyroid disease\...

\Hypothyroidism\Congenital hypothyroidism\Dyshormonogenic goitre\Thyroglobulin synthesis defect

\Inherited disorder of thyroid metabolism\Thyroglobulin synthesis defect

\Goitre\Dyshormonogenic goitre\Thyroglobulin synthesis defect

\Disorder of neck\Thyroid disease\...

\Hypothyroidism\Congenital hypothyroidism\Dyshormonogenic goitre\Thyroglobulin synthesis defect

\Inherited disorder of thyroid metabolism\Thyroglobulin synthesis defect

\Goitre\Dyshormonogenic goitre\Thyroglobulin synthesis defect

\Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Dyshormonogenic goitre\Thyroglobulin synthesis defect
\Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited disorder of thyroid metabolism\Thyroglobulin synthesis defect
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of endocrine system\Dyshormonogenic goitre\Thyroglobulin synthesis defect
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of endocrine system\Inherited disorder of thyroid metabolism\Thyroglobulin synthesis defect
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of endocrine system\Dyshormonogenic goitre\Thyroglobulin synthesis defect
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of endocrine system\Inherited disorder of thyroid metabolism\Thyroglobulin synthesis defect
\Disease\Disorder of body system\Disorder of endocrine system\Hereditary disorder of endocrine system\Dyshormonogenic goitre\Thyroglobulin synthesis defect
\Disease\Disorder of body system\Disorder of endocrine system\Hereditary disorder of endocrine system\Inherited disorder of thyroid metabolism\Thyroglobulin synthesis defect
\Disease\Disorder of body system\Disorder of endocrine system\Thyroid disease\Hypothyroidism\Congenital hypothyroidism\Dyshormonogenic goitre\Thyroglobulin synthesis defect
\Disease\Disorder of body system\Disorder of endocrine system\Thyroid disease\Inherited disorder of thyroid metabolism\Thyroglobulin synthesis defect
\Disease\Disorder of body system\Disorder of endocrine system\Thyroid disease\Goitre\Dyshormonogenic goitre\Thyroglobulin synthesis defect
\Disease\Disorder of neck\Thyroid disease\Hypothyroidism\Congenital hypothyroidism\Dyshormonogenic goitre\Thyroglobulin synthesis defect
\Disease\Disorder of neck\Thyroid disease\Inherited disorder of thyroid metabolism\Thyroglobulin synthesis defect
\Disease\Disorder of neck\Thyroid disease\Goitre\Dyshormonogenic goitre\Thyroglobulin synthesis defect
\Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Dyshormonogenic goitre\Thyroglobulin synthesis defect
\Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited disorder of thyroid metabolism\Thyroglobulin synthesis defect
\Disease\Congenital disease\Congenital hypothyroidism\Dyshormonogenic goitre\Thyroglobulin synthesis defect
\Disease\Congenital disease\Inborn error of metabolism\Dyshormonogenic goitre\Thyroglobulin synthesis defect
\Disease\Congenital disease\Inborn error of metabolism\Inherited disorder of thyroid metabolism\Thyroglobulin synthesis defect

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

104935010 Thyroglobulin synthesis defect en Synonym Active Case insensitive SNOMED CT core
104936011 Hypothyroidism due to thyroglobulin biosynthetic defect en Synonym Active Case insensitive SNOMED CT core
104937019 Genetic defect in thyroid hormonogenesis V en Synonym Active Initial character case insensitive SNOMED CT core
104938012 GDTH V en Synonym Inactive Case sensitive SNOMED CT core
499490011 Hypothyroidism due to thyroglobulin synthesis defect en Synonym Active Case insensitive SNOMED CT core
802376015 Thyroglobulin synthesis defect (disorder) en Fully specified name Active Case insensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Thyroglobulin synthesis defect	Interprets	Thyroid hormone measurement	false	Inferred relationship	Some	3
Thyroglobulin synthesis defect	Has interpretation	Above reference range	false	Inferred relationship	Some	3
Thyroglobulin synthesis defect	Finding site	Entire thyroid gland	true	Inferred relationship	Some	1
Thyroglobulin synthesis defect	Associated morphology	Enlargement	true	Inferred relationship	Some	1
Thyroglobulin synthesis defect	Occurrence	Congenital	false	Inferred relationship	Some
Thyroglobulin synthesis defect	Is a	Inherited disorder of thyroid metabolism	true	Inferred relationship	Some
Thyroglobulin synthesis defect	Is a	Hypothyroidism	false	Inferred relationship	Some
Thyroglobulin synthesis defect	Is a	Dyshormonogenic goitre	true	Inferred relationship	Some
Thyroglobulin synthesis defect	Associated morphology	Hyperplasia	false	Inferred relationship	Some	1
Thyroglobulin synthesis defect	Associated morphology	Hyperplasia	false	Inferred relationship	Some	1
Thyroglobulin synthesis defect	Finding site	Thyroid structure	false	Inferred relationship	Some	1
Thyroglobulin synthesis defect	Associated morphology	Enlargement	false	Inferred relationship	Some	2
Thyroglobulin synthesis defect	Finding site	Entire thyroid gland	false	Inferred relationship	Some	2
Thyroglobulin synthesis defect	Is a	Congenital hypothyroidism	false	Inferred relationship	Some
Thyroglobulin synthesis defect	Occurrence	Congenital	true	Inferred relationship	Some	1
Thyroglobulin synthesis defect	Finding site	Entire endocrine gonad	false	Inferred relationship	Some
Thyroglobulin synthesis defect	Finding site	Thyroid structure	false	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

REPLACED BY association reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
104935010	Thyroglobulin synthesis defect	en	Synonym	Active	Case insensitive	SNOMED CT core
104936011	Hypothyroidism due to thyroglobulin biosynthetic defect	en	Synonym	Active	Case insensitive	SNOMED CT core
104937019	Genetic defect in thyroid hormonogenesis V	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
104938012	GDTH V	en	Synonym	Inactive	Case sensitive	SNOMED CT core
499490011	Hypothyroidism due to thyroglobulin synthesis defect	en	Synonym	Active	Case insensitive	SNOMED CT core
802376015	Thyroglobulin synthesis defect (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core